Abiusi, Emanuela
 Distribuzione geografica
Continente #
EU - Europa 353
NA - Nord America 348
AS - Asia 90
AF - Africa 9
Totale 800
Nazione #
US - Stati Uniti d'America 343
SE - Svezia 140
IT - Italia 75
DE - Germania 56
CN - Cina 49
IE - Irlanda 27
TR - Turchia 11
FI - Finlandia 10
FR - Francia 10
IR - Iran 10
CI - Costa d'Avorio 9
UA - Ucraina 9
GB - Regno Unito 8
NL - Olanda 8
IN - India 7
KR - Corea 5
HK - Hong Kong 4
SG - Singapore 3
CH - Svizzera 2
CR - Costa Rica 2
AT - Austria 1
CA - Canada 1
CZ - Repubblica Ceca 1
ES - Italia 1
HR - Croazia 1
LI - Liechtenstein 1
MX - Messico 1
NO - Norvegia 1
PA - Panama 1
RS - Serbia 1
RU - Federazione Russa 1
VN - Vietnam 1
Totale 800
Città #
Chandler 93
Ashburn 40
Dublin 25
New York 24
Milan 23
Izmir 10
Nanchang 10
San Mateo 10
Abidjan 9
Boston 9
Nanjing 9
Wilmington 9
Jacksonville 8
Marseille 8
Cattolica 7
Helsinki 7
Houston 7
Princeton 7
Rome 7
Norwalk 6
Old Bridge 6
Bremen 5
Dearborn 5
Fairfield 5
Seoul 5
Augusta 4
Beijing 4
Hong Kong 4
Naaldwijk 4
Shenyang 4
Alcamo 3
Amsterdam 3
Caorle 3
Hefei 3
Munich 3
Nürnberg 3
Redwood City 3
Tehran 3
Tianjin 3
Trivandrum 3
Woodbridge 3
Bologna 2
Brixen 2
Cagliari 2
Cambridge 2
Ciserano 2
Cornate d'Adda 2
Fremont 2
Jinan 2
La Cruz 2
Lawrence 2
Los Angeles 2
Pisa 2
Salò 2
Seattle 2
Taizhou 2
Turin 2
Zurich 2
Andover 1
Atlanta 1
Boardman 1
Brno 1
Changchun 1
Changsha 1
Costa Mesa 1
Council Bluffs 1
Edinburgh 1
Frankfurt am Main 1
Fuzhou 1
Groningen 1
Guangzhou 1
Hangzhou 1
Hanoi 1
Hebei 1
Juarez 1
Kish 1
Kocaeli 1
Kragujevac 1
Kunming 1
Leipzig 1
London 1
Madrid 1
Mountain View 1
Nuremberg 1
Nutley 1
Oslo 1
Pune 1
Ranica 1
Saint Louis 1
San Diego 1
San Francisco 1
Singapore 1
Stockholm 1
Toronto 1
Udine 1
University Park 1
Verona 1
Vienna 1
Washington 1
Würzburg 1
Totale 483
Nome #
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study Running title: adult SMA biomarker study 143
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 87
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: Clues from a biomarker study 78
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol 65
Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screening 64
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy 62
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 58
Longitudinal assessments in discordant twins with SMA 55
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 52
Plasma miR-151-3p as a candidate diagnostic biomarker for head and neck cancer: a cross-sectional study within the INHANCE consortium 45
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: towards specific guidelines and standard operating procedures for the molecular diagnosis 39
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 20
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 9
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome 9
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: Towards specific guidelines and standard operating procedures for the molecular diagnosis 8
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis 8
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita 8
270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands 7
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome? 6
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene 4
Totale 827
Categoria #
all - tutte 4.351
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.351


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201931 0 0 0 0 0 0 0 0 0 0 10 21
2019/202049 15 2 0 0 4 3 14 2 3 0 4 2
2020/202129 0 2 0 3 3 1 8 1 4 4 3 0
2021/2022122 7 2 7 14 5 5 0 13 10 6 22 31
2022/2023319 53 39 12 30 36 20 37 36 28 7 14 7
2023/2024188 8 48 7 18 14 37 33 3 1 19 0 0
Totale 827